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一个编码MRPL12的延迟早期反应核基因,它是细菌翻译调节因子L7/L12蛋白的线粒体同源物。

A delayed-early response nuclear gene encoding MRPL12, the mitochondrial homologue to the bacterial translational regulator L7/L12 protein.

作者信息

Marty L, Fort P

机构信息

Institut de Génétique Moléculaire, UMR5535, CNRS-Universités Montpellier I et II, France.

出版信息

J Biol Chem. 1996 May 10;271(19):11468-76. doi: 10.1074/jbc.271.19.11468.

Abstract

We have characterized a new delayed-early response mRNA encoding a 21-kDa product (MRPL12) that accumulates during the G1 phase of growth-stimulated cells. MRPL12 is the mammalian homologue to chloroplastic and bacterial L12 ribosomal proteins. Immunofluorescence microscopy and cell fractionation indicate a predominant mitochondrial localization in various mammalian cell lines. The NH2-terminal 49 amino acids are necessary and sufficient to target the protein within the mitochondria and are probably cleaved off during import. MRPL12 proteins associated in vitro and cofractionate with ribosomal structures, as is the case for prokaryotic L12 proteins. Expression of a dominant inhibitory truncated protein leads to a severe reduction in cell growth by inhibiting mitochondrial ATP production. MRPL12 is the first mammalian mitochondrial ribosomal protein to be characterized.

摘要

我们鉴定了一种新的延迟早期反应mRNA,其编码一种21 kDa的产物(MRPL12),该产物在生长刺激细胞的G1期积累。MRPL12是叶绿体和细菌L12核糖体蛋白的哺乳动物同源物。免疫荧光显微镜和细胞分级分离表明,在各种哺乳动物细胞系中,MRPL12主要定位于线粒体。NH2末端的49个氨基酸对于将蛋白质靶向线粒体是必需且足够的,并且可能在导入过程中被切除。MRPL12蛋白在体外与核糖体结构相关联并共分级分离,原核L12蛋白也是如此。显性抑制性截短蛋白的表达通过抑制线粒体ATP产生导致细胞生长严重减少。MRPL12是第一个被鉴定的哺乳动物线粒体核糖体蛋白。

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